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IL-6 and hsCRP predict cardiovascular mortality in patients with heart failure with preserved ejection fraction.
Berger, Martin; März, Winfried; Niessner, Alexander; Delgado, Graciela; Kleber, Marcus; Scharnagl, Hubert; Marx, Nikolaus; Schuett, Katharina.
Affiliation
  • Berger M; Department of Internal Medicine I; University Hospital Aachen, RWTH University, Aachen, Germany.
  • März W; Medical Clinic V (Nephrology, Hypertensiology, Rheumatology, Endocrinology, Diabetology) Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
  • Niessner A; Synlab Academy, Synlab Holding Deutschland, Mannheim, Germany.
  • Delgado G; Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
  • Kleber M; Medical Clinic V (Nephrology, Hypertensiology, Rheumatology, Endocrinology, Diabetology) Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
  • Scharnagl H; Medical Clinic V (Nephrology, Hypertensiology, Rheumatology, Endocrinology, Diabetology) Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
  • Marx N; SYNLAB MVZ Humangenetik Mannheim, Mannheim, Germany.
  • Schuett K; Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, Austria.
ESC Heart Fail ; 2024 Jul 14.
Article in En | MEDLINE | ID: mdl-39003598
ABSTRACT

AIMS:

Inflammation accompanies heart failure (HF) and elevated levels of inflammatory biomarkers are linked to new onset of HF. However, whether the prognostic relevance of inflammatory biomarkers is different in HF with reduced (HFrEF) and preserved ejection fraction (HFpEF) is unclear. The aim of the current study is to explore the role of inflammation on the mortality risk in patients with HF.

METHODS:

We analysed interleukin-6 and hsCRP levels by ELISA and immunonephelometry, respectively, in HFpEF and HFrEF patients referred for coronary angiography and assessed the prognostic value in the Ludwigshafen Risk and Cardiovascular Health (LURIC) study.

RESULTS:

HF was present in 1086 patients (N = 506 HFpEF; N = 580 HFrEF; mean age 65 ± 10 years; 28% female). Increasing IL-6 levels were significantly associated with increased CV mortality in HFpEF [1.5 (95% CI 1.1-2.2), P = 0.018] but not HFrEF [HR 1.3 (95% CI 1.0-1.7), P = 0.06] patients. High-sensitive CRP followed a similar pattern but failed to reach statistical significance after full-adjustment (HFpEF HR 1.4 95%C I 1.0-2.0; P = 0.065; HFrEF HR 1.0 95% CI 0.7-1.3; P = 0.800). Interaction analysis in patients stratified by IL-6 and N terminal pro brain natriuretic peptide (NT-proBNP) above and below the median revealed a stepwise increase in CV-mortality in HFpEF (P = 0.036) but not HFrEF patients (P = 0.220). To investigate the relationship between IL-6 and NT-proBNP, we assessed the genetic IL6-Receptor variant p.Asp358Ala (rs2228145) which is linked to impaired IL-6 receptor signalling. Homozygous carriers with HFpEF but not HFrEF exhibited significantly lower NT-pro-BNP levels compared with wildtype carriers (HFpEF 779 pg/mL ± 787 vs. 1180 pg/ mL ± 1532; P = 0.008; HFrEF 2289 pg/ mL ± 3439 vs. 2326 pg/ mL ± 3386; P = 0.94), raising the hypothesis that IL-6 signalling may play a pathophysiological role in HFpEF.

CONCLUSIONS:

These data suggest a predictive value of elevated IL-6 for CV-mortality in HFpEF but not in HFrEF patients.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: ESC Heart Fail Year: 2024 Type: Article Affiliation country: Germany

Full text: 1 Database: MEDLINE Language: En Journal: ESC Heart Fail Year: 2024 Type: Article Affiliation country: Germany